NDC 11084-113 United Labs Instant Foam
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 11084 - Deb Usa, Inc.
- 11084-113 - United Labs Instant Foam
Product Packages
NDC Code 11084-113-27
Package Description: 400 mL in 1 BOTTLE, PUMP
NDC Code 11084-113-40
Package Description: 47 mL in 1 BOTTLE, PUMP
Product Details
What is NDC 11084-113?
What are the uses for United Labs Instant Foam?
Which are United Labs Instant Foam UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- BENZALKONIUM (UNII: 7N6JUD5X6Y) (Active Moiety)
Which are United Labs Instant Foam Inactive Ingredients UNII Codes?
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:
- WATER (UNII: 059QF0KO0R)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- LAURAMINE OXIDE (UNII: 4F6FC4MI8W)
- EDETATE SODIUM (UNII: MP1J8420LU)
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
- D&C RED NO. 33 (UNII: 9DBA0SBB0L)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
- MAGNESIUM NITRATE (UNII: 77CBG3UN78)
- MAGNESIUM CHLORIDE (UNII: 02F3473H9O)
What is the NDC to RxNorm Crosswalk for United Labs Instant Foam?
- RxCUI: 1020365 - benzalkonium chloride 0.13 % Topical Foam
- RxCUI: 1020365 - benzalkonium chloride 1.3 MG/ML Topical Foam
* Please review the disclaimer below.
[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.
[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.
[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".